Editing Muscle cell

{{short description|Type of cell found in muscle tissue}}
{{Redirect2|Muscle fiber|Myofiber|protein structures inside cells|Myofibril}}
{{Infobox cell
| Name        = Muscle cell
| Latin       = myocytus
| Greek       =
| Image       = Synapse diag3.png
| Caption     = General structure of a [[Skeletal muscle|skeletal muscle cell]] and [[neuromuscular junction]]: {{ordered list |style=text-align: left; |[[Axon]] |[[Neuromuscular junction]] |[[Skeletal muscle#Skeletal muscle cells|Skeletal muscle fiber]] | [[Myofibril]]}}
| Width       =
| Image2      =
| Caption2    = 
| Location = [[Muscle]]
}}
A '''muscle cell''', also known as a '''myocyte''', is a mature contractile [[Cell (biology)|cell]] in the [[muscle]] of an animal.<ref name="MeSH">{{MeSH name|Myocytes}}</ref> In humans and other [[vertebrate]]s there are three types: [[skeletal muscle|skeletal]], [[smooth muscle|smooth]], and [[Cardiac muscle|cardiac]] (cardiomyocytes).<ref name="Brunet 2016">{{cite journal | last=Brunet | first=Thibaut | display-authors=etal | title=The evolutionary origin of bilaterian smooth and striated myocytes | journal=eLife | volume=5 | date=2016 | issn=2050-084X | doi=10.7554/elife.19607 | page=1| doi-access=free | pmc=5167519 }}</ref> A [[skeletal muscle cell]] is long and threadlike with [[multinucleated|many nuclei]] and is called a ''muscle fiber''.<ref name="Saladin2011">{{cite book |last1=Saladin |first1=Kenneth S. |title=Human anatomy |date=2011 |publisher=McGraw-Hill |location=New York |isbn=9780071222075 |pages=72–73 |edition=3rd}}</ref> Muscle cells develop from embryonic [[precursor cell]]s called [[myoblast]]s.<ref name="MeSH" />

Skeletal muscle cells form by [[cell fusion|fusion]] of myoblasts to produce [[multinucleated]] cells ([[syncytium|syncytia]]) in a process known as [[myogenesis]].<ref name=scott>{{cite journal|last1=Scott|first1=W|last2=Stevens|first2=J|last3=Binder-Macleod|first3=SA|title=Human skeletal muscle fiber type classifications.|journal=Physical Therapy|date=2001|volume=81|issue=11|pages=1810–1816|doi=10.1093/ptj/81.11.1810|pmid=11694174|url=http://ptjournal.apta.org/content/81/11/1810.full|url-status=dead|archive-url=https://web.archive.org/web/20150213021358/http://ptjournal.apta.org/content/81/11/1810.full|archive-date=2015-02-13|doi-access=free|url-access=subscription}}</ref><ref>{{cite web |url=https://www.researchgate.net/post/Does_anyone_know_why_skeletal_muscle_fibers_have_peripheral_nuclei_but_the_cardiomyocytes_not_What_are_the_functional_advantages |title=Does anyone know why skeletal muscle fibers have peripheral nuclei, but the cardiomyocytes not? What are the functional advantages? |url-status=live |archive-url=https://web.archive.org/web/20170919005558/https://www.researchgate.net/post/Does_anyone_know_why_skeletal_muscle_fibers_have_peripheral_nuclei_but_the_cardiomyocytes_not_What_are_the_functional_advantages |archive-date=2017-09-19 }}</ref> Skeletal muscle cells and cardiac muscle cells both contain [[myofibril]]s and [[sarcomere]]s and form a [[striated muscle tissue]].<ref name="opentext">{{cite web |title=Cardiac muscle tissue |date=6 March 2013 |url=https://opentextbc.ca/anatomyandphysiologyopenstax/chapter/cardiac-muscle-tissue/ |access-date=3 May 2021|last1=Betts |first1=J. Gordon |last2=Young |first2=Kelly A. |last3=Wise |first3=James A. |last4=Johnson |first4=Eddie |last5=Poe |first5=Brandon |last6=Kruse |first6=Dean H. |last7=Korol |first7=Oksana |last8=Johnson |first8=Jody E. |last9=Womble |first9=Mark |last10=Desaix |first10=Peter }}</ref>

Cardiac muscle cells form the [[cardiac muscle]] in the walls of the heart chambers, and have a single central [[Cell nucleus|nucleus]].<ref>{{cite web|title=Muscle tissues|url=http://www.botany.uwc.ac.za/sci_ed/grade10/mammal/muscle.htm|url-status=dead|archive-url=https://web.archive.org/web/20151013025029/http://www.botany.uwc.ac.za/sci_ed/grade10/mammal/muscle.htm|archive-date=13 October 2015|access-date=29 September 2015}}</ref> Cardiac muscle cells are joined to neighboring cells by [[intercalated disc]]s, and when joined in a visible unit they are described as a ''cardiac muscle fiber''.<ref name="RBHT">{{cite web |title=Atrial structure, fibers, and conduction |url=https://www.rbht.nhs.uk/sites/nhs/files/Education%20and%20training/Ho-%20Atrial%20structure%20%26%20fibres%2C%20conduction.pdf |access-date=5 June 2021}}</ref>

Smooth muscle cells control involuntary movements such as the [[peristalsis]] contractions in the [[esophagus]] and [[stomach]]. Smooth muscle has no myofibrils or sarcomeres and is therefore non-striated. Smooth muscle cells have a single nucleus.

==Structure==
The unusual [[Histology|microscopic anatomy]] of a muscle cell gave rise to its terminology. The [[cytoplasm]] in a muscle cell is termed the [[sarcoplasm]]; the [[smooth endoplasmic reticulum]] of a muscle cell is termed the [[sarcoplasmic reticulum]]; and the [[cell membrane]] in a muscle cell is termed the [[sarcolemma]].<ref name="Saladin2011A">{{cite book |last1=Saladin |first1=Kenneth S. |title=Human anatomy |date=2011 |publisher=McGraw-Hill |location=New York |isbn=9780071222075 |pages=244–246 |edition=3rd}}</ref> The sarcolemma receives and conducts stimuli.

===Skeletal muscle cells===
{{Main|Skeletal muscle fibers}}
[[File:Blausen 0801 SkeletalMuscle.png|thumb|Diagram of skeletal muscle fiber structure]]
Skeletal muscle cells are the individual contractile cells within a muscle and are more usually known as muscle fibers because of their longer threadlike appearance.<ref name="SEER">{{cite web |title=Structure of Skeletal Muscle {{!}} SEER Training |url=https://training.seer.cancer.gov/anatomy/muscular/structure.html |website=training.seer.cancer.gov}}</ref> Broadly there are two types of muscle fiber performing in [[muscle contraction]], either as slow twitch ([[Type I muscle fiber|type I]]) or fast twitch ([[Type II muscle fiber|type II]]).

A single muscle such as the [[biceps brachii]] in a young adult human male contains around 253,000 muscle fibers.<ref name="Klein">{{cite journal |last1=Klein |first1=CS |last2=Marsh |first2=GD |last3=Petrella |first3=RJ |last4=Rice |first4=CL |title=Muscle fiber number in the biceps brachii muscle of young and old men. |journal=Muscle & Nerve |date=July 2003 |volume=28 |issue=1 |pages=62–8 |doi=10.1002/mus.10386 |pmid=12811774|s2cid=20508198 }}</ref> Skeletal muscle fibers are the only muscle cells that are [[multinucleate]]d with the [[Cell nucleus|nuclei]] usually referred to as [[myonuclei]]. This occurs during [[myogenesis]] with the [[cell fusion|fusion]] of [[myoblast]]s each contributing a nucleus to the newly formed muscle cell or [[myotube]].<ref name="Cho">{{cite journal |last1=Cho |first1=CH |last2=Lee |first2=KJ |last3=Lee |first3=EH |title=With the greatest care, stromal interaction molecule (STIM) proteins verify what skeletal muscle is doing. |journal=BMB Reports |date=August 2018 |volume=51 |issue=8 |pages=378–387 |doi=10.5483/bmbrep.2018.51.8.128 |pmid=29898810|pmc=6130827 }}</ref> Fusion depends on muscle-specific proteins known as [[fusogen]]s called ''myomaker'' and ''myomerger''.<ref name="Prasad">{{cite journal |last1=Prasad |first1=V |last2=Millay |first2=DP |title=Skeletal muscle fibers count on nuclear numbers for growth. |journal=Seminars in Cell & Developmental Biology |date=2021-05-08 |volume=119 |pages=3–10 |doi=10.1016/j.semcdb.2021.04.015 |pmid=33972174|pmc=9070318 |s2cid=234362466 }}</ref>

A striated muscle fiber contains [[myofibril]]s consisting of long protein chains of [[myofilament]]s. There are three types of myofilaments: thin, thick, and elastic that work together to produce a [[muscle contraction]].<ref name=saladin /> The thin myofilaments are filaments of mostly [[actin]] and the thick filaments are of mostly [[myosin]] and they [[sliding filament mechanism|slide over each other]] to shorten the fiber length in a muscle contraction. The third type of myofilament is an elastic filament composed of [[titin]], a very large protein.

In [[Striated muscle tissue|striations of muscle bands]], myosin forms the dark filaments that make up the [[Sarcomere#Bands|A band]]. Thin filaments of actin are the light filaments that make up the [[Sarcomere#Bands|I band]]. The smallest contractile unit in the fiber is called the sarcomere which is a repeating unit within two [[Sarcomere#Bands|Z bands]]. The sarcoplasm also contains [[glycogen]] which provides energy to the cell during heightened exercise, and [[myoglobin]], the red pigment that stores oxygen until needed for muscular activity.<ref name=saladin>{{cite book|last1=Saladin|first1=K|title=Anatomy & Physiology: The Unity of Form and Function|date=2012|publisher=McGraw-Hill|location=New York|isbn=978-0-07-337825-1|pages=403–405|edition=6th}}</ref>

The [[sarcoplasmic reticulum]], a specialized type of [[endoplasmic reticulum#smooth endoplasmic reticulum|smooth endoplasmic reticulum]], forms a network around each myofibril of the muscle fiber. This network is composed of groupings of two dilated end-sacs called terminal cisternae, and a single [[T-tubule]] (transverse tubule), which bores through the cell and emerge on the other side; together these three components form the [[Triad (anatomy)|triads]] that exist within the network of the sarcoplasmic reticulum, in which each T-tubule has two terminal cisternae on each side of it. The sarcoplasmic reticulum serves as a reservoir for calcium ions, so when an action potential spreads over the T-tubule, it signals the sarcoplasmic reticulum to release calcium ions from the gated membrane channels to stimulate muscle contraction.<ref name=saladin /><ref>{{cite journal|last1=Sugi|first1=Haruo|last2=Abe|first2=T|last3=Kobayashi|first3=T|last4=Chaen|first4=S|last5=Ohnuki|first5=Y|last6=Saeki|first6=Y|last7=Sugiura|first7=S|last8=Guerrero-Hernandez|first8=Agustin|title=Enhancement of force generated by individual myosin heads in skinned rabbit psoas muscle fibers at low ionic strength|journal=PLOS ONE|date=2013|volume=8|issue=5|pages=e63658|doi=10.1371/journal.pone.0063658|pmid=23691080|pmc=3655179|bibcode=2013PLoSO...863658S|doi-access=free}}</ref>

In skeletal muscle, at the end of each muscle fiber, the outer layer of the sarcolemma combines with tendon fibers at the [[myotendinous junction]].<ref name="Charvet">{{cite journal |last1=Charvet |first1=B |last2=Ruggiero |first2=F |last3=Le Guellec |first3=D |title=The development of the myotendinous junction. A review. |journal=Muscles, Ligaments and Tendons Journal |date=April 2012 |volume=2 |issue=2 |pages=53–63 |pmid=23738275|pmc=3666507 }}</ref><ref name=Bentzinger2012>{{cite journal|last1=Bentzinger|first1=CF|last2=Wang|first2=YX|last3=Rudnicki|first3=MA|title=Building muscle: molecular regulation of myogenesis.|journal=Cold Spring Harbor Perspectives in Biology|date=1 February 2012|volume=4|issue=2|doi=10.1101/cshperspect.a008342|pmid=22300977|pages=a008342|pmc=3281568}}</ref> Within the muscle fiber pressed against the sarcolemma are multiply flattened [[myonuclei|nuclei]]; embryologically, this [[multinucleate]] condition results from multiple myoblasts fusing to produce each muscle fiber, where each myoblast contributes one nucleus.<ref name=saladin />

===Cardiac muscle cells===
{{Main|Cardiac muscle}}
The cell membrane of a [[cardiac muscle cell]] has several specialized regions, which may include the [[intercalated disc]], and [[transverse tubule]]s. The cell membrane is covered by a lamina coat which is approximately 50&nbsp; nm wide. The laminar coat is separable into two layers; the [[lamina densa]] and [[lamina lucida]]. In between these two layers can be several different types of ions, including [[calcium]].<ref name=ferrari>{{cite web|last1=Ferrari|first1=Roberto|title=Healthy versus sick myocytes: metabolism, structure and function|url=http://eurheartjsupp.oxfordjournals.org/content/ehjsupp/4/suppl_G/G1.full.pdf|website=oxfordjournals.org/en|publisher=Oxford University Press|access-date=12 February 2015|url-status=dead|archive-url=https://web.archive.org/web/20150219100248/http://eurheartjsupp.oxfordjournals.org/content/ehjsupp/4/suppl_G/G1.full.pdf|archive-date=19 February 2015}}</ref>

Cardiac muscle like the skeletal muscle is also striated and the cells contain myofibrils, myofilaments, and sarcomeres as the skeletal muscle cell.
The cell membrane is anchored to the cell's [[cytoskeleton]] by anchor fibers that are approximately 10&nbsp; nm wide.  These are generally located at the Z lines so that they form grooves and transverse tubules emanate. In cardiac myocytes, this forms a scalloped surface.<ref name=ferrari />

The cytoskeleton is what the rest of the cell builds off of and has two primary purposes; the first is to stabilize the topography of the intracellular components and the second is to help control the size and shape of the cell. While the first function is important for biochemical processes, the latter is crucial in defining the surface-to-volume ratio of the cell. This heavily influences the potential electrical properties of [[excitable cell]]s. Additionally, deviation from the standard shape and size of the cell can have a negative prognostic impact.<ref name=ferrari />

===Smooth muscle cells===
{{Main|Smooth muscle}}{{Further|Basal electrical rhythm}}
[[Smooth muscle cells]] are so-called because they have neither myofibrils nor sarcomeres and therefore no [[striated muscle tissue|striations]]. They are found in the walls of hollow [[organs]], including the [[stomach]], [[intestines]], [[urinary bladder|bladder]] and [[uterus]], in the walls of [[blood vessel]]s, and in the tracts of the [[Respiratory system|respiratory]], [[Urinary system|urinary]], and [[reproductive system]]s. In the [[eye]]s, the [[ciliary muscle]]s dilate and contract the [[iris (anatomy)|iris]] and alter the shape of the [[lens (anatomy)|lens]]. In the [[skin]], smooth muscle cells such as those of the [[arrector pili]] cause [[hair]] to stand erect in response to [[cold|cold temperature]] or [[fear]].<ref name="open">{{cite web |title=Smooth muscle |date=6 March 2013 |url=https://opentextbc.ca/anatomyandphysiologyopenstax/chapter/smooth-muscle/ |access-date=10 June 2021|last1=Betts |first1=J. Gordon |last2=Young |first2=Kelly A. |last3=Wise |first3=James A. |last4=Johnson |first4=Eddie |last5=Poe |first5=Brandon |last6=Kruse |first6=Dean H. |last7=Korol |first7=Oksana |last8=Johnson |first8=Jody E. |last9=Womble |first9=Mark |last10=Desaix |first10=Peter }}</ref>

Smooth muscle cells are spindle-shaped with wide middles, and tapering ends. They have a single nucleus and range from 30 to 200 [[Micrometre|micrometer]]s in length. This is thousands of times shorter than skeletal muscle fibers. The diameter of their cells is also much smaller which removes the need for [[T-tubule]]s found in striated muscle cells. Although smooth muscle cells lack sarcomeres and myofibrils they do contain large amounts of the contractile proteins actin and myosin. Actin filaments are anchored by [[Smooth muscle#Dense bodies|dense bodies]] (similar to the [[Sarcomere#Bands|Z discs]] in sarcomeres) to the sarcolemma.<ref name="open"/>

==Development{{anchor|Myonuclei}}==
{{Main|Myogenesis}}

A [[myoblast]] is an embryonic [[precursor cell]] that [[Cellular differentiation|differentiates]] to give rise to the different muscle cell types.<ref>page 395, Biology, Fifth Edition, Campbell, 1999</ref> Differentiation is regulated by [[myogenic regulatory factors]], including [[MyoD]], [[Myf5]], [[myogenin]], and [[MRF4]].<ref>{{cite journal |vauthors=Perry R, Rudnick M |title=Molecular mechanisms regulating myogenic determination and differentiation |journal=Front Biosci |volume=5 |pages=D750–67 |year= 2000|pmid=10966875 |doi=10.2741/Perry|doi-access=free }}</ref> [[GATA4]] and [[GATA6]] also play a role in myocyte differentiation.<ref name="pmid18400219">{{cite journal |vauthors=Zhao R, Watt AJ, Battle MA, Li J, Bandow BJ, Duncan SA |title=Loss of both GATA4 and GATA6 blocks cardiac myocyte differentiation and results in acardia in mice |journal=Dev. Biol. |volume=317 |issue=2 |pages=614–9 |date=May 2008 |pmid=18400219 |pmc=2423416 |doi=10.1016/j.ydbio.2008.03.013 }}</ref>

[[Skeletal muscle#Skeletal muscle cells|Skeletal muscle fibers]] are made when myoblasts fuse together; muscle fibers therefore are cells with [[Multinucleate|multiple nuclei]], known as [[myonuclei]], with each [[cell nucleus]] originating from a single myoblast. The fusion of myoblasts is specific to skeletal muscle, and not [[cardiac muscle]] or [[smooth muscle]].

Myoblasts in skeletal muscle that do not form muscle fibers [[Dedifferentiation|dedifferentiate]] back into [[myosatellite cell]]s. These satellite cells remain adjacent to a skeletal muscle fiber, situated between the sarcolemma and the basement membrane<ref>{{cite journal|last1=Zammit|first1=PS|last2=Partridge|first2=TA|last3=Yablonka-Reuveni|first3=Z|title=The skeletal muscle satellite cell: the stem cell that came in from the cold.|journal=Journal of Histochemistry and Cytochemistry|date=November 2006|volume=54|issue=11|pages=1177–91|pmid=16899758|doi=10.1369/jhc.6r6995.2006|doi-access=free}}</ref> of the [[endomysium]] (the connective tissue investment that divides the muscle fascicles into individual fibers). To re-activate myogenesis, the satellite cells must be stimulated to differentiate into new fibers.

Myoblasts and their derivatives, including satellite cells, can now be generated in vitro through [[directed differentiation]] of [[Induced pluripotent stem cells|pluripotent stem cells]].<ref name="pmid26237517">{{cite journal |vauthors = Chal J, Oginuma M, Al Tanoury Z, Gobert B, Sumara O, Hick A, Bousson F, Zidouni Y, Mursch C, Moncuquet P, Tassy O, Vincent S, Miyazaki A, Bera A, Garnier JM, Guevara G, Heston M, Kennedy L, Hayashi S, Drayton B, Cherrier T, Gayraud-Morel B, Gussoni E, Relaix F, Tajbakhsh S, Pourquié O|title = Differentiation of pluripotent stem cells to muscle fiber to model Duchenne muscular dystrophy |journal = [[Nat. Biotechnol.|Nature Biotechnology]]|date = August 2015|pmid = 26237517|doi = 10.1038/nbt.3297 |volume=33 |issue = 9 |pages=962–9|s2cid = 21241434 |url = http://www.hal.inserm.fr/inserm-01484878}} {{Closed access}}</ref>

[[Kindlin-2]] plays a role in developmental elongation during myogenesis.<ref name="pmid18611274">{{cite journal |vauthors=Dowling JJ, Vreede AP, Kim S, Golden J, Feldman EL |title=Kindlin-2 is required for myocyte elongation and is essential for myogenesis |journal=BMC Cell Biol. |volume=9 |pages=36 |year=2008 |pmid=18611274 |pmc=2478659 |doi=10.1186/1471-2121-9-36 |doi-access=free }}</ref>

==Function==
===Muscle contraction in striated muscle===
{{Main|Muscle contraction}}
[[File:Sliding Filament Mechanism Diagram.pdf|thumb| ]]

====Skeletal muscle contraction====
When [[Muscle contraction|contracting]], thin and thick filaments slide concerning each other by using [[adenosine triphosphate]].  This pulls the Z discs closer together in a process called the sliding filament mechanism.  The contraction of all the [[sarcomeres]] results in the contraction of the whole muscle fiber. This contraction of the myocyte is triggered by the [[action potential]] over the [[cell membrane]] of the myocyte. The action potential uses [[transverse tubules]] to get from the surface to the interior of the myocyte, which is continuous within the cell membrane.
Sarcoplasmic reticula are membranous bags that transverse tubules touch but remain separate from. These wrap themselves around each sarcomere and are filled with Ca<sup>2+</sup>.<ref name="courses.washington.edu">{{cite web|title=Structure, and Function of Skeletal Muscles|url=http://courses.washington.edu/conj/motor/musclereview.htm|website=courses.washington.edu|access-date=13 February 2015|url-status=live|archive-url=https://web.archive.org/web/20150215092857/http://courses.washington.edu/conj/motor/musclereview.htm|archive-date=15 February 2015}}</ref>

Excitation of a myocyte causes depolarization at its synapses, the [[neuromuscular junctions]], which triggers an action potential. With a singular neuromuscular junction, each muscle fiber receives input from just one somatic efferent neuron. Action potential in a somatic efferent neuron causes the release of the neurotransmitter [[acetylcholine]].<ref>{{cite web|title=Muscle Fiber Excitation|url=http://courses.washington.edu/conj/bess/muscle/musclexcitation.html|website=courses.washington.edu|publisher=University of Washington|access-date=11 February 2015|url-status=live|archive-url=https://web.archive.org/web/20150227010858/http://courses.washington.edu/conj/bess/muscle/musclexcitation.html|archive-date=27 February 2015}}</ref>

When the acetylcholine is released it diffuses across the [[synapse]] and binds to a receptor on the [[sarcolemma]], a term unique to muscle cells that refers to the cell membrane. This initiates an impulse that travels across the sarcolemma.<ref name=ziser>{{cite web|last1=Ziser|first1=Stephen|title=Muscle Cell Anatomy & Function|url=http://www.austincc.edu/sziser/Biol%202404/2404LecNotes/2404LNExII/Muscle%20Physiology.pdf|website=www.austincc.edu|access-date=12 February 2015|url-status=live|archive-url=https://web.archive.org/web/20150923181106/http://www.austincc.edu/sziser/Biol%202404/2404LecNotes/2404LNExII/Muscle%20Physiology.pdf|archive-date=23 September 2015}}</ref>

When the action potential reaches the sarcoplasmic reticulum it triggers the release of Ca<sup>2+</sup> from the Ca<sup>2+</sup> channels. The Ca<sup>2+</sup> flows from the sarcoplasmic reticulum into the sarcomere with both of its filaments. This causes the filaments to start sliding and the sarcomeres to become shorter. This requires a large amount of ATP, as it is used in both the attachment and release of every [[myosin]] head. Very quickly Ca<sup>2+</sup> is actively transported back into the sarcoplasmic reticulum, which blocks the interaction between the thin and thick filament. This in turn causes the muscle cell to relax.<ref name=ziser />

There are four main [[Muscle contraction#Types|types of muscle contraction]]: isometric, isotonic, eccentric and concentric.<ref name="Gash">{{cite web |last1=Gash |first1=Matthew C. |last2=Kandle |first2=Patricia F. |last3=Murray |first3=Ian V. |last4=Varacallo |first4=Matthew |title=Physiology, Muscle Contraction |url=https://www.ncbi.nlm.nih.gov/books/NBK537140/ |website=StatPearls |publisher=StatPearls Publishing |date=2024}}</ref>  [[Isometric contraction]]s are skeletal muscle contractions that do not cause movement of the muscle. and [[isotonic contraction]]s are skeletal muscle contractions that do cause movement. [[Eccentric training|Eccentric contraction]] is when a muscle moves under a load. Concentric contraction is when a muscle shortens and generates force.

====Cardiac muscle contraction====
{{See also|Bowditch effect}}
Specialized [[cardiomyocytes]] in the [[sinoatrial node]] generate electrical impulses that control the [[heart]] rate.  These electrical impulses coordinate contraction throughout the remaining heart muscle via the [[electrical conduction system of the heart]].  Sinoatrial node activity is modulated, in turn, by nerve fibers of both the [[Sympathetic nervous system|sympathetic]] and [[Parasympathetic nervous system|parasympathetic]] nervous systems.  These systems act to increase and decrease, respectively, the rate of production of electrical impulses by the sinoatrial node.

== Evolution ==
{{Further|Evolution|Adaptation}}
The [[evolution]]ary origin of muscle cells in [[animals]] is highly debated: One view is that muscle cells evolved once, and thus all muscle cells have a single common ancestor. Another view is that muscles cells evolved more than once, and any [[Morphological convergence|morphological]] or structural similarities are due to [[convergent evolution]], and the development of shared genes that predate the evolution of muscle – even the [[mesoderm]] (the [[germ layer]]) that gives rise to muscle cells in vertebrates).

Schmid & Seipel (2005)<ref name="Seipel and Schmid"/> argue that the origin of muscle cells is a [[monophyletic]] trait that occurred concurrently with the development of the digestive and nervous systems of all animals, and that this origin can be traced to a single metazoan ancestor in which muscle cells are present. They argue that molecular and morphological similarities between the muscles cells in [[non-bilaterian]] [[Cnidaria]] and [[Ctenophora]], are similar enough to those of [[bilateria]]ns that there would be one ancestor in metazoans from which muscle cells derive. In this case, Schmid & Seipel argue that the last common ancestor of Bilateria, Ctenophora and Cnidaria, was a [[Triploblasty|triploblast]] (an organism having three germ layers), and that [[diploblasty]], meaning an organism with two germ layers, evolved secondarily, because of their observation of the lack of mesoderm or muscle found in most cnidarians and ctenophores. By comparing the morphology of cnidarians and ctenophores to bilaterians, Schmid & Seipel were able to conclude that there were [[myoblast]]-like structures in the tentacles and gut of some species of cnidarians and the tentacles of ctenophores. Since this is a structure unique to muscle cells, these scientists determined based on the data collected by their peers that this is a marker for [[Striated muscle tissue|striated muscles]] similar to that observed in bilaterians. The authors also remark that the muscle cells found in cnidarians and ctenophores are often contested due to the origin of these muscle cells being the [[ectoderm]] rather than the mesoderm or mesendoderm.

The origin of true muscle cells is argued by other authors to be the [[endoderm]] portion of the [[mesoderm]] and the endoderm. However, Schmid & Seipel (2005)<ref name="Seipel and Schmid"/> counter skepticism – about whether the muscle cells found in ctenophores and cnidarians are "true" muscle cells – by considering that cnidarians develop through a medusa stage and polyp stage. They note that in the hydrozoans' medusa stage, there is a layer of cells that separate from the distal side of the ectoderm, which forms the striated muscle cells in a way similar to that of the mesoderm; they call this third separated layer of cells the ''ectocodon''. Schmid & Seipel argue that, even in bilaterians, not all muscle cells are derived from the mesendoderm: Their key examples are that in both the eye muscles of vertebrates and the muscles of spiralians, these cells derive from the ectodermal mesoderm, rather than the endodermal mesoderm. Furthermore, they argue that since myogenesis does occur in cnidarians with the help of the same molecular regulatory elements found in the specification of muscle cells in bilaterians, that there is evidence for a single origin for striated muscle.<ref name="Seipel and Schmid">{{cite journal |first1 = Katja |last1 = Seipel |first2 = Volker |last2 = Schmid |date = 1 June 2005 |title = Evolution of striated muscle: Jellyfish and the origin of triploblasty |journal = Developmental Biology |volume = 282 |issue = 1 |pages = 14–26 |pmid=15936326 |doi = 10.1016/j.ydbio.2005.03.032 |doi-access = free}}</ref>

In contrast to this argument for a single origin of muscle cells, Steinmetz, Kraus, ''et al''. (2012)<ref name="independent evolution"/> argue that molecular markers such as the [[Myosin|myosin II]] protein used to determine this single origin of striated muscle predate the formation of muscle cells. They use an example of the contractile elements present in the Porifera, or sponges, that do truly lack this striated muscle containing this protein. Furthermore, Steinmetz, Kraus, ''et al''. present evidence for a [[Polyphyly|polyphyletic]] origin of striated muscle cell development through their analysis of morphological and molecular markers that are present in bilaterians and absent in cnidarians, ctenophores, and bilaterians. Steinmetz, Kraus, ''et al''. showed that the traditional morphological and regulatory markers such as [[actin]], the ability to couple myosin side chains phosphorylation to higher concentrations of the positive concentrations of calcium, and other [[Myosin|MyHC]] elements are present in all metazoans not just the organisms that have been shown to have muscle cells. Thus, the usage of any of these structural or regulatory elements in determining whether or not the muscle cells of the cnidarians and ctenophores are similar enough to the muscle cells of the bilaterians to confirm a single lineage is questionable according to Steinmetz, Kraus, ''et al''. Furthermore, they explain that the orthologues of the Myc genes that have been used to hypothesize the origin of striated muscle occurred through a gene duplication event that predates the first true muscle cells (meaning striated muscle), and they show that the Myc genes are present in the sponges that have contractile elements but no true muscle cells. Steinmetz, Kraus, ''et al''. also showed that the localization of this duplicated set of genes that serve both the function of facilitating the formation of striated muscle genes, and cell regulation and movement genes, were already separated into striated much and non-muscle MHC. This separation of the duplicated set of genes is shown through the localization of the striated much to the contractile vacuole in sponges, while the non-muscle much was more diffusely expressed during developmental cell shape and change. Steinmetz, Kraus, ''et al''. found a similar pattern of localization in cnidarians except with the cnidarian ''N.&nbsp;vectensis'' having this striated muscle marker present in the smooth muscle of the digestive tract. Thus, they argue that the pleisiomorphic trait of the separated orthologues of much cannot be used to determine the monophylogeny of muscle, and additionally argue that the presence of a striated muscle marker in the smooth muscle of this cnidarian shows a fundamental different mechanism of muscle cell development and structure in cnidarians.<ref name="independent evolution">{{cite journal |first1 = Patrick R.H. |last1 = Steinmetz |first2 = Johanna E.M. |last2 = Kraus |first3 = Claire |last3 = Larroux |first4 = Jörg U. |last4 = Hammel |first5 = Annette |last5 = Amon-Hassenzahl |first6 = Evelyn |last6 = Houliston |first7 = Gert |last7 = Wörheide |first8 = Michael |last8 = Nickel |first9 = Bernard M. |last9 = Degnan |display-authors = 6 |year = 2012 |title = Independent evolution of striated muscles in cnidarians and bilaterians |journal = Nature |volume = 487 |issue = 7406 |pages = 231–234 |pmc = 3398149 |pmid = 22763458 |doi = 10.1038/nature11180 |bibcode = 2012Natur.487..231S}}</ref>

Steinmetz, Kraus, ''et al''. (2012)<ref name="independent evolution"/> further argue for multiple origins of striated muscle in the metazoans by explaining that a key set of genes used to form the troponin complex for muscle regulation and formation in bilaterians is missing from the cnidarians and ctenophores, and 47&nbsp;structural and regulatory proteins observed, Steinmetz, Kraus, ''et al''. were not able to find even on unique striated muscle cell protein that was expressed in both cnidarians and bilaterians. Furthermore, the Z-disc seemed to have evolved differently even within bilaterians and there is a great deal of diversity of proteins developed even between this clade, showing a large degree of radiation for muscle cells. Through this divergence of the [[Sarcomere|Z-disc]], Steinmetz, Kraus, ''et al''. argue that there are only four common protein components that were present in all bilaterians muscle ancestors and that of these for necessary Z-disc components only an actin protein that they have already argued is an uninformative marker through its pleisiomorphic state is present in cnidarians. Through further molecular marker testing, Steinmetz et al. observe that non-bilaterians lack many regulatory and structural components necessary for bilaterians muscle formation and do not find any unique set of proteins to both bilaterians and cnidarians and ctenophores that are not present in earlier, more primitive animals such as the sponges and [[amoebozoa]]ns. Through this analysis, the authors conclude that due to the lack of elements that bilaterian muscles are dependent on for structure and usage, nonbilaterian muscles must be of a different origin with a different set of regulatory and structural proteins.<ref name="independent evolution"/>

In another take on the argument, Andrikou & Arnone (2015)<ref name=myogenesis/> use the newly available data on [[gene regulatory network]]s to look at how the hierarchy of genes and morphogens and another mechanism of tissue specification diverge and are similar among early deuterostomes and protostomes. By understanding not only what genes are present in all bilaterians but also the time and place of deployment of these genes, Andrikou & Arnone discuss a deeper understanding of the evolution of myogenesis.<ref name=myogenesis/>

In their paper, Andrikou & Arnone (2015)<ref name=myogenesis/> argue that to truly understand the evolution of muscle cells the function of transcriptional regulators must be understood in the context of other external and internal interactions. Through their analysis, Andrikou & Arnone found that there were conserved [[orthologues]] of the gene regulatory network in both invertebrate bilaterians and cnidarians. They argue that having this common, general regulatory circuit allowed for a high degree of divergence from a single well-functioning network. Andrikou & Arnone found that the orthologues of genes found in vertebrates had been changed through different types of structural mutations in the invertebrate deuterostomes and protostomes, and they argue that these structural changes in the genes allowed for a large divergence of muscle function and muscle formation in these species. Andrikou & Arnone were able to recognize not only any difference due to mutation in the genes found in vertebrates and invertebrates but also the integration of species-specific genes that could also cause divergence from the original gene regulatory network function. Thus, although a common muscle patterning system has been determined, they argue that this could be due to a more ancestral gene regulatory network being coopted several times across lineages with additional genes and mutations causing very divergent development of muscles. Thus it seems that the myogenic patterning framework may be an ancestral trait. However, Andrikou & Arnone explain that the basic muscle patterning structure must also be considered in combination with the [[Cis-Regulatory element|cis regulatory elements]] present at different times during development. In contrast with the high level of gene family apparatuses structure, Andrikou and Arnone found that the cis-regulatory elements were not well conserved both in time and place in the network which could show a large degree of divergence in the formation of muscle cells. Through this analysis, it seems that the myogenic GRN is an ancestral GRN with actual changes in myogenic function and structure possibly being linked to later coopts of genes at different times and places.<ref name=myogenesis>{{Cite journal |first1 = Carmen |last1 = Andrikou |first2 = Maria Ina |last2 = Arnone |title = Too many ways to make a muscle: Evolution of GRNs governing myogenesis |journal = Zoologischer Anzeiger |date = 1 May 2015 |volume = 256 |pages = 2–13 |series = Special Issue: Proceedings of the 3rd International Congress on Invertebrate Morphology |doi = 10.1016/j.jcz.2015.03.005}}</ref>

Evolutionarily, specialized forms of skeletal and [[cardiac muscle]]s predated the divergence of the [[vertebrate]] / [[arthropod]] evolutionary line.<ref name=evolution>{{cite journal |last1=OOta |first1=S. |last2=Saitou |first2=N. |year=1999 |title=Phylogenetic relationship of muscle tissues deduced from the superimposition of gene trees |journal=Molecular Biology and Evolution |volume=16 |issue=6 |pages=856–867 |issn=0737-4038 |doi=10.1093/oxfordjournals.molbev.a026170 |doi-access=free |pmid=10368962}}</ref> This indicates that these types of muscle developed in a common [[ancestor]] sometime before 700&nbsp;[[mya (unit)|million years ago (mya)]]. Vertebrate smooth muscle was found to have evolved independently from the skeletal and cardiac muscle types.

=== Invertebrate muscle cell types ===
The properties used for distinguishing fast, intermediate, and slow muscle fibers can be different for invertebrate flight and jump muscle.<ref name="Hoyle 1983">{{cite book | last=Hoyle | first=Graham | year=1983  | chapter=8. Muscle cell diversity | title=Muscles and Their Neural Control | publisher=John Wiley & Sons | location=New York, NY | pages=[https://archive.org/details/musclestheirneur0000hoyl/page/293 293–299] | isbn=9780471877097 | chapter-url=https://archive.org/details/musclestheirneur0000hoyl/page/293 }}</ref> To further complicate this classification scheme, the mitochondrial content, and other morphological properties within a muscle fiber, can change in a [[tsetse fly]] with exercise and age.<ref name="Anderson, M., and Finlayson, L. H. 1976">{{cite journal | last1 = Anderson | first1 = M. | last2 = Finlayson | first2 = L.H. | year = 1976 | title = The effect of exercise on the growth of mitochondria and myofibrils in the flight muscles of the Tsetse fly, Glossina morsitans | journal = J. Morphol. | volume = 150 | issue = 2 | pages = 321–326 | doi = 10.1002/jmor.1051500205 | s2cid = 85719905 }}</ref>

== See also ==
* [[List of human cell types derived from the germ layers]]
* [[List of distinct cell types in the adult human body]]

== References ==
{{Reflist}}

==External links==
* {{Commons category-inline|Myocytes}}
* [http://www.ivy-rose.co.uk/HumanBody/Muscles/Muscle_Cell.php Structure of a Muscle Cell]

{{Muscle tissue}}
{{Authority control}}
{{Use dmy dates|date=November 2019}}

[[Category:Contractile cells]]
[[Category:Animal cells]]
[[Category:Non-terminally differentiated (blast) cells]]
[[Category:Myoblasts|*]]